HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064745Generated: October 25, 2026
Sodium Carbonate → 4'-Methoxy-3-methyl-1,1'-biphenyl-4-carbonitrile
https://huagongshe.com/reaction/1064745
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromo-2-methylbenzonitrile | HCID 144267 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4'-Methoxy-3-methyl-1,1'-biphenyl-4-carbonitrile | HCID 11218346 | 102.7% |
Reaction Steps
4-Bromo-2-methylbenzonitrile (4.9 g, 25.0 mmol), Pd(PPh3)4 (578 mg) in benzene (50 mL) and 2.0 M aqueous solution of Na2CO3 (25 mL, 50.0 mmol) was treated with 4-methoxyphenylboronic acid (4.56 g, 30.0 mmol) in ethanol (20 mL) and heated at 75° C. for 17 hours. The mixture was allowed to cool to room temperature and the phases were separated. The aqueous phase was extracted with diethyl ether (3×40 mL). The original benzene layer and the diethyl ether extracts were combined, filtered over celite, dried over sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by chromatography over silica using a mixture of hexane/CH2Cl2 (3:1) to provide the title compound as a white powder (5.73 g, 85% yield). 1HNMR (300 MHz, CDCl3) δ 2.35 (3H), 3.70 (s, 3H), 6.80-7.50 (m, 7H); MS (DCI) m/z 224 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06969730B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-e29f2c73feb0419498af6bf12b410522 |
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| Source note | uspto-grants-2005_11 |
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